Bhatia R, Srivastava MVP, Khurana D, Pandit L, Mathew T, Gupta S, Netravathi M, Nair SS, Singh G, Singhal BS. Consensus Statement On Immune Modulation in Multiple Sclerosis and Related Disorders During the COVID-19 Pandemic: Expert Group on Behalf of the Indian Academy of Neurology. Ann Indian Acad Neurol. 2020 Apr;23(Suppl 1):S5-S14.
Nair SS, Harikrishnan S, Sarma PS, Thomas SV. Metabolic syndrome in young adults with epilepsy. Seizure 2016;37:61-4.
Wadwekar V, Nair SS, Tandon V, Kuruvilla A, Nair M. Congenital myasthenic syndrome: Ten years clinical experience from a quaternary care south-Indian hospital. J Clin Neurosci. 2-019. https://doi.org/10.1016/j.jocn.2019.11.030
Sundaram S, Nair SS, Jaganmohan D, Unnikrishnan G, Nair M. Relapsing lumbosacral myeloradiculitis: An unusual presentation of MOG antibody disease. Mult Scler. 2019 1:1352458519840747. doi: 10.1177/1352458519840747.
Wadwekar V, Pillai RR, Sesh S, Nair SS, Nair MD. Pregnancy-associated respiratory failure in MuSK-congenital myasthenic syndrome. Muscle Nerve 2019;59(4):E24-E26.
Neelima R, Krishnakumar K, Nair MD, Kesavadas C, Hingwala DR, Radhakrishnan VV, Nair SS. Tumefactive demyelinating lesions: A clinicopathological correlative study. Indian Journal of Pathology and Microbiology 2012;55:496-500
Sylaja PN, Srivastava MVP, Shah S, Bhatia R, Khurana D, Sharma A, Pandian JD, Kalia K, Sarmah D, Nair SS, Yavagal DR, Bhattacharya P. The SARS-CoV-2/COVID-19 pandemic and challenges in stroke care in India. Ann N Y Acad Sci. 2020 May 12:10.1111/nyas.14379. doi: 10.1111/nyas.14379.
Karunakaran S, Menon RN, Nair SS, Santhakumar S, Nair M, Sundaram S. Clinical and Genetic Profile of Autism Spectrum Disorder-Epilepsy (ASD-E) Phenotype: Two Sides of the Same Coin! Clin EEG Neurosci. 2020 Nov;51(6):390-398. doi: 10.1177/1550059420909673
Nambiar PN, Kumar S S, Menon R, Nair SS, Madhavilatha GK, Sundaram S. Horizontal gaze palsy and progressive scoliosis-a tale of two siblings with ROBO3 mutation. Ophthalmic Genet. 2020 Feb;41(1):99-100. doi: 10.1080/13816810.2020.1727537
Vinayagamani S, Nair SS, Sundaram S. Teaching Neuroimages: Hypomyelinating leukodystrophy with generalized dystonia. Neurology. 2020;94(3):e335-e336.
Vedartham V, Sundaram S, Nair SS, Ganapathy A, Mannan A, Menon R. Homozygous sequestosome 1 (SQSTM1) mutation: a rare cause for childhood-onset progressive cerebellar ataxia with vertical gaze palsy. Ophthalmic Genet. 2019;40:376-9.
Raina A, Nair SS, Nagesh C, Thomas B, Nair M, Sundaram S. Electroneurography and advanced neuroimaging profile in pediatric-onset metachromatic leukodystrophy. 2019. Journal of Pediatric Neurosciences.2019;14(2):70-5.
Vysakha KV, Poyuran R, Nair SS, Nair M. An unusual presentation of scleromyxedema as inflammatory myopathy. Acta Myologica. 2019; 38 (1):13
Menon D, Nair SS, Thomas B, Krishnakumar K, Nair M. Clinico-radiological correlation and surgical outcome of idiopathic spinal cord herniation: A single centre retrospective case series. The Journal of Spinal Cord Medicine 2019. DOI: 10.1080/10790268.2019.1579986.
Sruthi SN, Sylaja PN. Initial stroke severity and stroke outcome ??? the inseparable link. Neurol India 2017;65:1260-1.
Nair SS, Sylaja PN, Sapna ES, Sarma PS. Maintenance of normoglycemia may improve outcome in acute ischemic stroke. Ann Indian Acad Neurol. 2017;20:122-6.
Menon D, Nair SS, Kuruvilla A, Nair MD. Ophthalmoplegia in young onset amyotrophic lateral sclerosis: A case report and review of literature. Curr Neurobiol 2017; 8: 14-19
Nair SS, Arathy JS, Jayakumar RM, Sreedharan SE, Sylaja PN. Persistent post stroke dysphagia treated with cricopharyngeal myotomy: a case report. Ann Indian Acad Neurol 2016; 19: 249-51.
Cyril AC, Nair SS, Mathai A, Sudheeran K, Thomas SV. Autoimmune encephalitis: Clinical diagnosis versus antibody confirmation. Ann Indian Acad Neurol 2015;18:408-411
Jagtap SA, Nair SS, Jain N, Nair MD. Rapidly progressive dementia, Parkinsonism and myoclonus: An unusual presentation of dural arteriovenous fistula. Neurology India 2014;62:107- 10.